Micromed BRAIN QUICK system— 510(k) K171384
Substantially EquivalentMicromed S.P.A.
FDA 510(k) clearance K171384 for Micromed BRAIN QUICK system, Substantially Equivalent on 2018-02-01. Applicant: Micromed S.P.A.. Device class: 2.
Clearance details
- Applicant
- Micromed S.P.A.
- Product code
- Code GWQ
- Device class
- Class 2
- Regulation
- 21 CFR 882.1400
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mogliano Veneto, IT
Recent devices under product code GWQ
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view allRecalls naming K171384
K-number listed on FDA's recall recordMatched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K171384.
Data sourced from openFDA. This site is unofficial and independent of the FDA.